ausblenden:
Schlagwörter:
SINGLE-MOLECULE FRET; STRUCTURAL INSIGHTS; CRYSTAL-STRUCTURE; LIGAND
EFFICACY; ARRESTIN; RECONSTITUTION; AGONISTS; TARGETS
Zusammenfassung:
G-protein-coupled receptors (GPCRs) mediate a wide range of human physiological functions by transducing extracellular ligand binding events into intracellular responses. GPCRs can activate parallel, independent signaling pathways mediated by G proteins or beta-arrestins. Whereas "balanced'' agonists activate both pathways equally, "biased'' agonists dominantly activate one pathway, which is of interest for designing GPCR-targeting drugs because it may mitigate undesirable side effects. Previous studies demonstrated that beta-arrestin activation is associated with transmembrane helix VII (TM VII) of GPCRs. Here, single-molecule fluorescence spectroscopy with the beta(2)-adrenergic receptor (beta(2)AR) in the ligand-free state showed that TM VII spontaneously fluctuates between one inactive and one active-like conformation. The presence of the beta-arrestin-biased agonist isoetharine prolongs the dwell time of TM VII in the active-like conformation compared with the balanced agonist formoterol, suggesting that ligands can induce signaling bias by modulating the kinetics of receptor conformational exchange.
